European Journal of Radiology 55 (2005) 452–460
High resolution computed tomographic features of
pulmonary alveolar microlithiasis
Omer Deniz
∗
, Fatih Ors, Ergun Tozkoparan, Ayhan Ozcan, Seyfettin Gumus, Ugur Bozlar,
Hayati Bilgic, Kudret Ekiz, Necmettin Demirci
Pulmonary Medicine and Tuberculosis, Gulhane Military Medical Academy, Etlik, Ankara 06018, Turkey
Received 11 October 2004; received in revised form 3 January 2005; accepted 5 January 2005
Abstract
Background: Pulmonary alveolar microlithiasis (PAM) is a rare, chronic lung disease with unknown etiology and with a nonuniform clinical
course. Nonuniformity of clinical course might be related to the degree of pulmonary parenchymal alterations, which can be revealed with
high resolution computed tomography (HRCT). However, HRCT findings of PAM were not fully described in the current literature.
Aim: The aim of this study was to interpret and to contribute to describe HRCT findings of PAM and to investigate a correlation between
profusion of micro nodules (MN) and pulmonary parenchymal alterations in patients with PAM.
Material and methods: Ten male patients with PAM (mean age: 22 ± 3.2) were included into the study. HRCT images were assessed for
patterns, distribution, and profusion of pulmonary abnormalities. Dividing the lungs into three zones, profusion of abnormalities was assessed.
A profusion score (1–4) was given and the scores of each zone were then summed to obtain a global profusion score for HRCT ranging from
0 to 12. Also a parenchymal alteration score (PAS) was defined with respect to profusion of abnormalities. Chest X-rays were also scored.
Results: All of ten patients with PAM had findings of interstitial lung disease in varying degrees on their HRCTs. HRCT findings of patients
with PAM were as following: MN, parenchymal bands (PB), ground glass opacity (GGO) and, sub pleural interstitial thickening (SPIT) in 10
patients; interlobular septal thickening (ILST), in 9 patients; paraseptal emphysema (PSA) in 8 patients; centrilobular emphysema (CLA) in 7
patients; bronchiectasis (BE), confluent micro nodules (CMN) in 6 patients; peri bronchovascular interstitial thickening (PBIT) in 5 patients;
panacinar emphysema (PANAA) in 3 patients; pleural calcification (PC) in 2 patients.
A significant correlation between MN scores and PAS (r = 0.68, p = 0.031, MN scores and GGO scores (r = 0.69, p = 0.027) and, MN scores
and CLA scores (r = 0.67, p = 0.034) was detected.
We also found significant correlations between HRCT scores and results of pulmonary function tests (PFTs), HRCT scores and chest X-ray
score (CXRS) and, CXRS and results of PFTs.
Conclusion: We conclude that patients with PAM may have all findings of interstitial lung disease in varying degrees as well as MNs on their
HRCTs. More importantly, this study suggests a proportional relationship between profusion of MNs and parenchymal alterations in patients
with PAM. This study also suggests that the degree of parenchymal alterations closely related with the degree of pulmonary function loss in
patients with PAM.
© 2005 Elsevier Ireland Ltd. All rights reserved.
Keywords: Alveolar microlithiasis; HRCT; Radiology
1. Introduction
Pulmonary alveolar microlithiasis (PAM) is a rare, chronic
lung disease with unknown etiology characterized by exten-
∗
Corresponding author. Tel.: +90 312 3044406; fax: +90 312 3042700.
E-mail address: odeniz@gata.edu.tr (O. Deniz).
sive intra-alveolar spherical calcium and phosphate deposi-
tion throughout both lung parenchymas.
The incidence of PAM is high in certain countries such
as Turkey, Italy and USA [1,2]. Patients with PAM usually
show sand like micro nodular infiltration particularly marked
at lower zones predominantly at para cardiac areas in their
chest X-rays. Since there is a surprising discordance between
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doi:10.1016/j.ejrad.2005.01.010